Evidence map›Paper›PMID 40211768›Full record

ReviewImmunological reviews2025

Transcriptional Regulation of Mouse Mast Cell Differentiation and the Role of Human Lung Mast Cells in Airway Inflammation.

Junfeng Gao, Dianzheng Zhao, Hamid Reza Nouri, Hong Wei Chu, Hua Huang

Abstract readReview
In one paragraph

Review in Immunological reviews, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Crosstalk Between Allergic Inflammation and Autophagy.International journal of molecular sciences · 2025
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Junfeng GaoDepartment of Immunology and Genomic Medicine, National Jewish Health, Denver, Colorado, USA.ORCID 0000-0001-5098-5993
Dianzheng ZhaoDepartment of Immunology and Genomic Medicine, National Jewish Health, Denver, Colorado, USA.
Hamid Reza NouriDepartment of Medicine, National Jewish Health, Denver, Colorado, USA.
Hong Wei ChuDepartment of Medicine, National Jewish Health, Denver, Colorado, USA.
Hua HuangDepartment of Immunology and Genomic Medicine, National Jewish Health, Denver, Colorado, USA.ORCID 0000-0001-7317-8983

Funding

Tollip inhibits IL-33 signaling during airway influenza virus infectionU19AI125357 · NIAID · UNIVERSITY OF ARIZONA · PI CHU, HONG W · 2016 to 2025
$14.7M
Parkin in mitochondrial dysfunction and airway inflammation of obese asthmaR01AI152504 · NIAID · NATIONAL JEWISH HEALTH · PI CHU, HONG W, HOLGUIN, FERNANDO · 2020 to 2024
$3.7M
Novel Biased Beta2-AR Ligands as Asthma TherapeuticsR01AI161296 · NIAID · DUKE UNIVERSITY · PI CHU, HONG W, DICKEY, BURTON F · 2021 to 2025
$3.2M
Role of immunoproteasome in airway viral infectionR01AI150082 · NIAID · NATIONAL JEWISH HEALTH · PI CHU, HONG W · 2020 to 2024
$2.8M
Innate Effectors and Type-2 InflammationR01AI107022 · NIAID · NATIONAL JEWISH HEALTH · PI HUANG, HUA · 2016 to 2020
$2.0M
Gene Responses in Basophil-Mediated Allergic ResponsesR01AI083986 · NIAID · NATIONAL JEWISH HEALTH · PI HUANG, HUA · 2010 to 2014
$1.9M
Mast Cell Lineage Commitment and FunctionR01AI182277 · NIAID · NATIONAL JEWISH HEALTH · PI HUA HUANG · 2025 to 2026
$1.2M
Transcriptional Regulation of the Il13 Gene in Mast CellsR56AI180204 · NIAID · NATIONAL JEWISH HEALTH · PI HUANG, HUA · 2024 to 2024
$252k
NIAID NIH HHS R01 AI083986NIAID NIH HHS R01 AI107022NIAID NIH HHS R01 AI150082NIAID NIH HHS R01 AI152504NIAID NIH HHS R01 AI161296NIAID NIH HHS R01 AI182277NIAID NIH HHS R56 AI180204NIAID NIH HHS U19 AI125357NIH HHS R01AI083986NIH HHS R01AI107022NIH HHS R01AI150082NIH HHS R01AI152504NIH HHS R01AI161296NIH HHS U19AI125357
6 · The paper itself

Abstract

Mast cells (MCs) play a critical role in allergic inflammation, anaphylaxis, and chronic inflammatory diseases such as asthma, COPD, and osteoarthritis. Dysregulated MC activation can lead to MC activation syndrome (MACS), which is observed in patients with long COVID. MCs express the high-affinity receptor for IgE and, upon activation, release mediators and cytokines that trigger anaphylactic shock and promote allergic inflammation. They also interact with epithelial and nerve cells, which are crucial in forming a complex network of cell-cell and gene-gene interactions driving chronic inflammation that can confer resistance to treatment. In this review, in the context of the literature, we focus on experiments conducted in our laboratory investigating how transcription factors and enhancers regulate genes critical in mouse MC differentiation and function related to human lung inflammation.

Indexed as

COVID-19LungMast CellsSARS-CoV-2AnimalsCell DifferentiationGene Expression RegulationHumansInflammationMiceTranscription FactorsTranscription Factorsenhancerslung inflammationmast cell genesmast cell progenitorstranscriptional cooperationtranscription factors

Identifiers

PMID40211768
PMCPMC12017346

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.